Technical Field
[0001] The present invention relates to a polymerizable phosphorylcholine group-containing
polysiloxane monomer that may be used for producing an ophthalmic device, such as
a contact lens, an intraocular lens, or an artificial cornea, by being copolymerized
with a hydrophilic monomer and the like.
[0002] The present application claims priority from Japanese Patent Application No.
2018-073052, which is incorporated herein by reference.
Background Art
[0003] A silicone hydrogel is a material that puts little strain on the eyes by virtue of
its high oxygen permeability, and that is hence currently widely used for ophthalmic
lenses, such as contact lenses. Meanwhile, the silicone hydrogel contains a water-repellent
silicone, and hence is liable to lack wettability or lubricity. Therefore, investigations
have been made on surface hydrophilization by a surface modification method and surface
hydrophilization by mixing a hydrophilic polymer into a lens composition before curing
thereof. At present, there exist various methods of providing a silicone hydrogel
lens that has optical transparency and desired lubricity, allows adjustment of an
elastic modulus, and has high oxygen permeability.
[0004] During wearing of the silicone hydrogel lens, a protein, a lipid, or the like in
a tear serves as a cause of deterioration of wearing sensation by being adsorbed onto
a surface of the lens. For the purpose of reducing the adsorption thereof, a lens
using a phosphorylcholine group-containing methacrylic ester monomer MPC having contamination
resistance (Patent Literature 1 and Non Patent Literature 1) is commercially available
as a non-silicone hydrogel lens.
[0005] In Patent Literature 2, there is a disclosure that a phosphorylcholine group, which
has contamination resistance, is incorporated into a silicone hydrogel lens. In Patent
Literature 2, there is a disclosure of a silicone hydrogel produced by random copolymerization
of 2-methacryloylethylphosphorylcholine (MPC) and bis(trimethylsiloxy)methylsilylpropylglycerol
methacrylate (SiGMA), which is a polysiloxane monomer having a hydroxy group.
[0006] In general, when MPC is used by being copolymerized in the introduction of a phosphorylcholine
group into a silicone hydrogel lens, there is a need to overcome phase separation
between a highly hydrophilic MPC moiety and a hydrophobic silicone moiety in a silicone
hydrogel backbone. Accordingly, there still remains room for improvement in stable
production of silicone hydrogel lenses, and it is important to design a polysiloxane
monomer having introduced therein a phosphorylcholine group.
[0007] In Patent Literature 3, there is a disclosure of a polysiloxane monomer having phosphorylcholine-analogous
groups introduced at both ends of a silicone chain. In addition, in each of Patent
Literature 4 and Patent Literature 5, there is a disclosure of a polysiloxane monomer
having phosphorylcholine groups introduced at both ends thereof. In each of the polysiloxane
monomers having those structures, a polydimethylsiloxane moiety of a main chain is
not modified, and hence it cannot necessarily be said that sufficient performance
is obtained in terms of compatibility with a hydrophilic monomer and transparency
of a lens to be obtained. Accordingly, there is room for improvement.
[0008] In Patent Literature 6, there is a disclosure of an ABA-type MPC/siloxane block polymer.
The block polymer is extremely useful when used for surface treatment. However, when
the block polymer is used as a crosslinker for a lens, its block structure results
in a large phase-separated structure of a hydrophilic phase and a hydrophobic layer,
and hence there is a risk in that the hydrogel is liable to be clouded.
[0009] In Patent Literature 7, there is a disclosure of a silicone having a phosphorylcholine
group introduced into a silicone side chain thereof via an amino group. Despite having
the phosphorylcholine group, the silicone cannot necessarily be said to be safe owing
to the presence of the amino group.
[0010] In Patent Literature 8, there is a proposal of a polysiloxane monomer having a phosphorylcholine
group introduced via an ester group. Owing to having the ester group, the monomer
cannot be said to have high compatibility with a hydrophilic monomer, such as 2-hydroxyethyl
(meth)acrylate, which has a hydroxy group.
Citation List
Patent Literature
Non Patent Literature
Summary of Invention
Technical Problem
[0013] The present invention provides a phosphorylcholine group-containing polysiloxane
monomer that shows high surface hydrophilicity, a high oxygen transmissibility, and
appropriate mechanical physical properties (particularly suitable for application
to an ophthalmic device) when copolymerized with a polymerizable monomer, such as
a hydrophilic monomer.
Solution to Problem
[0014] The inventors of the present invention have recognized that a phosphorylcholine group-containing
polysiloxane monomer represented by the formula (1) can solve the problems. Thus,
the present invention has been completed.
[0015] In the formula, "a" represents an integer of from 20 to 500, "b" represents an integer
of from 1 to 70, "c" represents 0 or 1, "p" and "q" each represent 0 or 1, and X represents
- CH
2- or -CH
2CH
2-.
[0016] That is, the present invention is as described below.
- 1. A phosphorylcholine group-containing polysiloxane monomer, which is represented
by the formula (1):
where "a" represents an integer of from 20 to 500, "b" represents an integer of from
1 to 70, "c" represents 0 or 1, "p" and "q" each represent 0 or 1, and X represents
-CH2- or CH2CH2-.
- 2. A method of producing a phosphorylcholine group-containing polysiloxane monomer
represented by the formula (1), the method including a step of subjecting a hydrosilyl
group-containing di-methacrylate-terminated silicone represented by the formula (4)
and an allyl group-containing phosphorylcholine compound represented by the formula
(5) to an addition reaction:
where "a" represents an integer of from 20 to 500, "b" represents an integer of from
1 to 70, "c" represents 0 or 1, "p" and "q" each represent 0 or 1, and X represents
-CH2- or CH2CH2-;
where "a" represents an integer of from 20 to 500, "b" represents an integer of from
1 to 70, and "p" and "q" each represent 0 or 1;
where "c" represents 0 or 1, and Z represents CH2=CHCH2- or CH2=CH-.
- 3. A monomer composition, including: 10 parts by weight to 60 parts by weight of a
phosphorylcholine group-containing polysiloxane monomer represented by the formula
(1) ; and 40 parts by weight to 90 parts by weight of one kind or a plurality of kinds
of hydrophilic monomers:
where "a" represents an integer of from 20 to 500, "b" represents an integer of from
1 to 70, "c" represents 0 or 1, "p" and "q" each represent 0 or 1, and X represents
-CH2- or CH2CH2-.
- 4. The monomer composition according to the above-mentioned item 3, wherein the hydrophilic
monomers are any one or more selected from the group consisting of 2-hydroxyethyl
(meth)acrylate, N-vinylpyrrolidone, N,N-dimethylacrylamide, 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl)
phosphate, methyl methacrylate, and hydroxypropyl (meth)acrylate.
- 5. A polymer, which is obtained by polymerizing the monomer composition of the above-mentioned
item 3 or 4.
- 6. A polymer, which is obtained by polymerizing the monomer composition of the above-mentioned
item 3 or 4, wherein the hydrophilic monomers are N-vinylpyrrolidone, 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl)
phosphate, and hydroxypropyl (meth)acrylate.
- 7. A polymer, which is obtained by polymerizing the monomer composition of the above-mentioned
item 3 or 4, wherein the hydrophilic monomers are N-vinylpyrrolidone, 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl)
phosphate, and 2-hydroxyethyl (meth)acrylate.
- 8. A polymer, which is obtained by polymerizing the monomer composition of the above-mentioned
item 3 or 4, wherein the hydrophilic monomers are N-vinylpyrrolidone, 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl)
phosphate, and N,N-dimethylacrylamide.
- 9. The composition according to any one of the above-mentioned items 1 to 4, wherein
the composition is a composition for an ophthalmic device.
- 10. An ophthalmic device, including the polymer of any one of the above-mentioned
items 5 to 8.
Advantageous Effects of Invention
[0017] The phosphorylcholine group-containing polysiloxane monomer of the present invention
has a high silicone content and has high hydrophilicity by virtue of having a phosphorylcholine
group. Accordingly, the phosphorylcholine group-containing polysiloxane monomer simultaneously
satisfies surface hydrophilicity, appropriate mechanical strength, and oxygen permeability
when copolymerized with a polymerizable monomer, such as a hydrophilic monomer, and
hence is useful as a polysiloxane monomer to be used as a raw material for an ophthalmic
device.
Description of Embodiments
[0018] The present invention relates to a polysiloxane monomer containing a phosphorylcholine
group, which is a zwitterionic group. More specifically, the polysiloxane monomer
containing a phosphorylcholine group of the present invention relates to a polymerizable
silicone compound containing a silicone moiety and further containing a zwitterionic
phosphorylcholine group in the molecule and two vinyl end groups, and having a number-average
molecular weight of from 2,000 to 50,000. The number-average molecular weight of the
polysiloxane monomer containing a phosphorylcholine group of the present invention
only needs to be from 2,000 to 50,000, and is preferably from 4,600 to 42,000.
[0019] The vinyl groups of the phosphorylcholine group-containing polysiloxane monomer of
the present invention are each adjacent to a carbonyl group. Accordingly, the phosphorylcholine
group-containing polysiloxane monomer has good copolymerizability with a monomer to
be generally used for an ophthalmic device, such as a (meth)acrylic ester monomer
or a (meth)acrylamide monomer.
[0020] The phosphorylcholine group-containing polysiloxane monomer of the present invention
has a phosphorylcholine moiety, which is a zwitterionic group, in a side chain thereof,
and hence has high compatibility with a hydrophilic monomer and provides a transparent
lens by being polymerized with the monomer. Further, surface hydrophilicity is achieved
in the lens, and hence the phosphorylcholine group-containing polysiloxane monomer
is also preferred as a crosslinker for contact lenses.
[0021] The term "ophthalmic device" as used in the present invention encompasses a contact
lens, a soft contact lens, a hard contact lens, an intraocular lens, and an artificial
cornea, but is not particularly limited thereto.
(Phosphorylcholine Group-containing Polysiloxane Monomer of the Present Invention)
[0022] The phosphorylcholine group-containing polysiloxane monomer of the present invention
is a phosphorylcholine group-containing polysiloxane monomer represented by the following
formula (1).
[0023] In the formula, "a" represents an integer of from 20 to 500, "b" represents an integer
of from 1 to 70, "c" represents 0 or 1, "p" and "q" each represent 0 or 1, and X represents
- CH
2- or -CH
2CH
2-.
[0024] "a" and "b" are not particularly limited as long as "a" and "b" fall within the above-mentioned
ranges. However, "a" represents from 20 to 500, preferably from 50 to 300, more preferably
from 80 to 200, and "b" represents from 1 to 70, preferably from 2 to 40, more preferably
from 3 to 15.
[0025] (Synthesis Method for Phosphorylcholine Group-containing Polysiloxane Monomer of
the Present Invention)
[0026] The phosphorylcholine group-containing polysiloxane monomer of the present invention
may be synthesized by any of various methods without any particular limitation. The
following method is given as an example.
[0027] A silicone intermediate represented by the formula (2) to be used for the synthesis
of the phosphorylcholine group-containing polysiloxane monomer of the present invention
may be synthesized by a known method.
[0028] A dual-end hydroxy group-containing siloxane represented by the following formula
(2) {e.g., SIB1138.0 from Gelest, Inc. (in the formula (2), p=q=1 and n=0)}, an end
hydroxy group-containing disiloxane, such as SIB1145.0 (in the formula (2), p=q=n=0),
a dual-end hydroxy group-containing silicone, such as FM-4411 from JNC Corporation
(in the formula (2), p=q=1 and n=9), or the like is allowed to react with (meth)acrylic
acid chloride in the coexistence of a dehydrochlorinating agent to synthesize a compound
having methacrylic groups at both ends thereof represented by the formula (3). An
organic amine may be used as the dehydrochlorinating agent. The following organic
amine is preferably used: a trialkylamine, such as triethylamine; a dialkylamine,
such as diisopropylamine; diazabicycloundecene; or the like. An aprotic solvent may
be used at the time of the reaction. Tetrahydrofuran is preferred from the viewpoint
of solubility.
In the formula, "p" and "q" each represent 0 or 1, and n represents an integer of
from 0 to 10.
In the formula, "p" and "q" each represent 0 or 1, and n represents an integer of
from 0 to 10.
[0029] The compound represented by the formula (3) may be purchased as, for example, FM-7711
from JNC Corporation (p=q=0 and n=9) or DMS-R11 from Gelest, Inc. (p=q=0 and n=9).
[0030] Next, the silicone intermediate having methacrylic groups represented by the formula
(3) is allowed to react with octamethylcyclotetrasiloxane and 1,3,5,7-tetramethylcyclotetrasiloxane
through use of, for example, an acid catalyst, such as trifluoromethanesulfonic acid,
to afford a hydrosilyl group-containing silicone intermediate (hydrosilyl group-containing
di-methacrylate-terminated silicone) represented by the formula (4). This reaction
may be solvent-free, or may use a solvent, such as chloroform.
[0031] In the formula, "a" represents an integer of from 20 to 500, "b" represents an integer
of from 1 to 70, and "p" and "q" each represent 0 or 1.
[0032] "a" and "b" are not particularly limited as long as "a" and "b" fall within the above-mentioned
ranges. However, "a" represents from 20 to 500, preferably from 50 to 300, more preferably
from 80 to 200, and "b" represents from 1 to 70, preferably from 2 to 40, more preferably
from 3 to 15.
[0033] The acid catalyst after the reaction is removed by a known method. For example, the
acid catalyst may be removed by washing with water or by adsorption with sodium carbonate
or the like.
[0034] Further, the hydrosilyl group-containing silicone intermediate represented by the
formula (4) and a phosphorylcholine group-containing allyl ether represented by the
formula (5) are subjected to a hydrosilylation reaction, which is an addition reaction.
An excess amount of the compound of the formula (5) is removed with a solvent or the
like, and low-boiling point components are removed under reduced pressure. Thus, the
phosphorylcholine group-containing polysiloxane monomer of the formula (1) is obtained.
[0035] The compound of the formula (5) is obtained by allowing ethylene glycol monoallyl
ether to react with 2-chloro-2-oxo-1,3,2-dioxaphospholane (COP) in an aprotic solvent,
such as THF, to afford 2-(2-allyloxy)ethoxy-2-oxo-1,3,2-dioxaphospholane, followed
by a reaction with trimethylamine in an aprotic solvent, such as acetonitrile.
[0036] In the formula, "c" represents 0 or 1, and Z represents CH
2=CHCH
2- or CH
2=CH-.
(Monomer Composition of the Present Invention)
[0037] A monomer composition of the present invention contains the phosphorylcholine group-containing
polysiloxane monomer of the present invention and at least one kind of hydrophilic
monomer.
[0038] The phosphorylcholine group-containing polysiloxane monomer represented by the formula
(1) contained in the monomer composition of the present invention may be polymerized
with the hydrophilic monomer and the like using a catalyst or initiator known to a
person skilled in the art.
[0039] In the monomer composition of the present invention, the content ratio of the phosphorylcholine
group-containing polysiloxane monomer represented by the formula (1) of the present
invention is from 10 parts by weight to 60 parts by weight with respect to 100 parts
by weight of the total amount of the compound of the formula (1) and the hydrophilic
monomer. When the content ratio is less than 10 parts by weight, the transparency
and oxygen permeability of the polymer to be obtained by the polymerization are reduced,
and when the content ratio is more than 60 parts by weight, the surface hydrophilicity
of the polymer is reduced.
[0040] In the monomer composition of the present invention, the content ratio of the hydrophilic
monomer is generally from 40 parts by weight to 90 parts by weight, preferably from
50 parts by weight to 90 parts by weight with respect to 100 parts by weight of the
total amount of the compound of the formula (1) and the hydrophilic monomer.
[0041] The phosphorylcholine group-containing polysiloxane monomer represented by the formula
(1) of the present invention may be used as a monomer raw material for a polymer for
forming an ophthalmic device, in order to improve the surface hydrophilicity of the
ophthalmic device and control the softness thereof. More specifically, the polysiloxane
monomer of the present invention has polymerizable groups at both ends thereof, and
hence the softness of the polymer can be adjusted by adjusting the molecular weight
of the monomer (a decrease in molecular weight of the monomer makes the polymer harder,
and an increase therein makes the polymer softer). In addition, the monomer may be
incorporated into a monomer composition for an ophthalmic device in the range of from
10 parts by weight to 60 parts by weight.
[0042] That is, a polymer may be formed by mixing the phosphorylcholine group-containing
polysiloxane monomer represented by the formula (1) of the present invention with
a monomer (in particular, a hydrophilic monomer) that is copolymerizable with the
former monomer and is preferably used as a raw material for an ophthalmic device.
[0043] In addition, when the polysiloxane monomer of the present invention is used as a
raw material for an ophthalmic device, the softness of the ophthalmic device can be
controlled.
(Hydrophilic Monomer)
[0044] The hydrophilic monomer may be selected, for example, from the group consisting of
2-hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate,
4-hydroxybutyl (meth)acrylate, 2-hydroxyethyl acrylamide, N-methyl-2-hydroxyethyl
acrylamide, ethylene glycol monovinyl ether, N-vinylpyrrolidone, N,N-dimethylacrylamide,
N,N-diethylacrylamide, 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl) phosphate
{2-(meth)acryloyloxyethyl-2'-(trimethylammonio)ethyl phosphate}, and mixtures thereof,
but is not particularly limited.
[0045] When a plurality of kinds of hydrophilic monomers are incorporated into the monomer
composition of the present invention, their combination is not particularly limited,
but may be exemplified by the following.
[0046] N-Vinylpyrrolidone (NVP), 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl) phosphate
(MPC), and hydroxypropyl (meth)acrylate (HPMA)
NVP, MPC, and 2-hydroxyethyl (meth)acrylate (HEMA)
NVP, MPC, and N,N-dimethylacrylamide (DMAA)
MPC, HPMA, and DMAA
(Other Monomer)
[0047] The monomer composition of the present invention may contain, in addition to the
above-mentioned essential monomers, another monomer copolymerizable with the phosphorylcholine
group-containing polysiloxane monomer represented by the formula (1) of the present
invention, and preferably usable as a raw material for an ophthalmic device.
[0048] Preferred examples of the other monomer include known monomers each having a carbon-carbon
unsaturated bond, such as a (meth)acryloyl group, a styryl group, an allyl group,
or a vinyl group. In particular, a monomer having a hydrophilic group, such as a hydroxy
group, an amide group, or a zwitterion group, other than the above-mentioned hydrophilic
monomer is particularly preferred. Alternatively, a crosslinker may be added as the
other monomer as long as the effects of the present invention are not impaired. There
are given, for example, 2-hydroxy-3-(tris(trimethylsiloxy)silyl)propyl methacrylate,
4-(2-hydroxyethyl)=1-[3-tris (trimethylsiloxy)silylpropyl]=2-methylidene succinate,
and tetraethylene glycol dimethacrylate.
[0049] The content ratio of the other monomer is generally 100 parts by weight or less,
preferably 60 parts by weight or less with respect to 100 parts by weight of the total
amount of the above-mentioned essential monomers (the compound of the formula (1)
and the hydrophilic monomer).
(Polymer of the Present Invention)
[0050] A polymer of the present invention is obtained by polymerizing the monomer composition
of the present invention.
[0051] The polymerization may be performed by a known method with a thermal polymerization
initiator, which is typified by a peroxide or an azo compound, or a photopolymerization
initiator being appropriately added.
[0052] When thermal polymerization is performed, a thermal polymerization initiator having
a decomposition characteristic optimal for a desired reaction temperature may be selected
and used. That is, a peroxide or azo compound having a 10-hour half-life temperature
of from 40°C to 120°C is suitable. An example of the azo compound is 2,2'-azobis(isobutyronitrile)
(AIBN).
[0053] Examples of the photopolymerization initiator may include a carbonyl compound, a
sulfur compound, a halogen compound, and a metal salt.
[0054] Those polymerization initiators may be used alone or as a mixture thereof, and are
preferably used at a ratio of from 0.2 part by weight to 2 parts by weight with respect
to 100 parts by weight of the total amount of the compound of the formula (1) of the
present invention and the hydrophilic monomer.
[0055] The synthesis of the polymer of the present invention may be performed in the presence
of a solvent. The solvent may be any solvent that dissolves the monomer composition
and does not react therewith, and examples thereof may include water, an alcohol-based
solvent, a ketone-based solvent, an ester-based solvent, a linear or cyclic ether-based
solvent, and a nitrogen-containing solvent. A preferred example is water or an alcohol,
or a mixed solvent thereof.
[0056] Examples of the alcohol-based solvent include hexanol (HexOH), methanol, ethanol,
n-propanol, and isopropanol.
[0057] Examples of the ketone-based solvent include acetone, methyl ethyl ketone, and diethyl
ketone.
[0058] An example of the ester-based solvent is ethyl acetate.
[0059] Examples of the linear or cyclic ether-based solvent include ethyl cellosolve and
tetrahydrofuran.
[0060] Examples of the nitrogen-containing solvent include acetonitrile and N-methylpyrrolidone.
[0061] The polymer of the present invention may be a polymer obtained by polymerizing any
one of the following combinations of monomers.
[0062] The phosphorylcholine group-containing polysiloxane monomer of the present invention;
2-(methacryloyloxyethyl)-2-(trimethylammonioethyl) phosphate (MPC), hydroxypropyl
methacrylate (HPMA), and N-vinylpyrrolidone (NVP) each serving as the hydrophilic
monomer; and 2-hydroxy-3-(tris(trimethylsiloxy)silyl)propyl methacrylate (SiGMA) and
tetraethylene glycol dimethacrylate (TEGDMA) each serving as the other monomer
[0063] The phosphorylcholine group-containing polysiloxane monomer of the present invention;
MPC, HPMA, and NVP each serving as the hydrophilic monomer; and 4-(2-hydroxyethyl)=1-[3-tris(trimethylsiloxy)silylpropyl]=2-methylidene
succinate (ES) and TEGDMA each serving as the other monomer
[0064] The phosphorylcholine group-containing polysiloxane monomer of the present invention;
MPC, NVP, and 2-hydroxyethyl methacrylate (HEMA) each serving as the hydrophilic monomer;
and SiGMA and TEGDMA each serving as the other monomer
[0065] The phosphorylcholine group-containing polysiloxane monomer of the present invention;
MPC, NVP, and N,N-dimethylacrylamide (DMAA) each serving as the hydrophilic monomer;
and ES and TEGDMA each serving as the other monomer
[0066] The phosphorylcholine group-containing polysiloxane monomer of the present invention;
MPC, HPMA, and DMAA each serving as the hydrophilic monomer; and ES and TEGDMA each
serving as the other monomer
[0067] When the polymer of the present invention is obtained by polymerizing the phosphorylcholine
group-containing polysiloxane monomer of the present invention, the hydrophilic monomer,
and the other monomer, a weight ratio among the phosphorylcholine group-containing
polysiloxane monomer, the hydrophilic monomer, and the other monomer is not particularly
limited, but may be set to, for example, 10 to 60:40 to 90:0.01 to 60.
[0068] The present invention also encompasses a method of producing an ophthalmic device,
including the following steps:
- (I) a step of mixing the phosphorylcholine group-containing polysiloxane monomer of
the present invention with at least a hydrophilic monomer to obtain a monomer composition;
and
- (II) a step of polymerizing the monomer composition obtained in the step (I) to obtain
a polymer.
[0069] The monomer composition of the step (I) may further contain another monomer.
[0070] The production method may further include the following step:
(III) a step of removing an unreacted component.
[0071] The phosphorylcholine group-containing polysiloxane monomer of the present invention
may be used as a raw material for an ophthalmic device.
[0072] The ophthalmic device contains the polymer of the present invention.
[0073] The ophthalmic device is not particularly limited as long as the ophthalmic device
is one to be used for an eye of an animal including a human. For example, the ophthalmic
device may be a contact lens, a soft contact lens, a hard contact lens, an intraocular
lens, or an artificial cornea, and is preferably a soft contact lens.
Examples
[0074] Now, the present invention is described in more detail by way of Examples and Comparative
Examples, but the present invention is not limited thereto.
[0075] [Synthesis Example 1] Synthesis of Allyl Group-containing Phosphorylcholine Compound
represented by Formula (5)
[0076] In a 1 L four-necked flask, 97.26 g (0.68 mol) of 2-chloro-2-oxo-1,3,2-dioxaphospholane
(COP) was dissolved in 389.03 g of acetonitrile, and the whole was cooled to 5°C or
less in an ice bath. A solution obtained by dissolving 66.38 g (0.65 mol) of ethylene
glycol monoallyl ether (manufactured by Tokyo Chemical Industry Co., Ltd.) and 69.07
g (0.68 mol) of triethylamine (manufactured by Kishida Chemical Co., Ltd.) in 135.45
g of acetonitrile in a 500 mL beaker was transferred to a 300 mL dropping funnel,
and added dropwise into the previously prepared COP solution over 1 hour. Further,
a reaction was performed in an ice bath for 4 hours. Triethylamine hydrochloride produced
by the reaction was separated by filtration, and then 61.46 g (1.04 mol) of trimethylamine
was loaded. The mixture was subjected to a reaction at 75°C for 8 hours. After cooling,
the produced target product was separated by filtration, and washed with 140 g of
acetone twice. The solvent was removed under reduced pressure to afford 104.1 g of
the product. It was confirmed by
1H NMR that the product was the compound of the formula (5) ("c" represented 1, and
Z represented CH
2=CHCH
2-).
[0077] [Synthesis Example 2] Synthesis of Hydrosilyl Group-containing Di-methacrylate-terminated
Silicone represented by Formula (4)
[0078] In a 500 mL light-shielding bottle, 17.24 g of FM-7711 (JNC Corporation, bi-terminal
methacryloyloxypropylpolydimethylsiloxane (molecular weight≈1,000)), 150.0 g of octamethylcyclotetrasiloxane,
6.74 g of 1,3,5,7-tetramethylcyclotetrasiloxane, and 173.99 g of chloroform were mixed,
and 1.50 g of trifluoromethanesulfonic acid was further added. The mixture was subjected
to a reaction at 25°C for 8 hours, and then washed with about 1,500 g of ion-exchanged
water 5 times. After that, low-boiling components were removed under reduced pressure,
24.2 g of acetone and 120.1 g of methanol were added, and the whole was stirred. After
the mixture had been left to stand still, an upper layer was discarded, and a lower
layer was placed under reduced pressure to evaporate low-boiling components to afford
127.09 g of a transparent liquid. It was confirmed by
1H NMR that the liquid was the hydrosilyl group-containing silicone intermediate of
the formula (4) (referred to as silicone intermediate 1).
1H NMR Analysis Values
Peak area values for 2H of end double bonds at 5.54 ppm and 6.10 ppm (1.00+1.01=2.01)
An area value for 9H derived from a hydrosilyl group at 4.68 ppm (4.88)
A peak area value derived from siloxane at 0.16 ppm (651.67)
[0079] Calculation from the above-mentioned values found the following: a≈108, b=5, p=0,
and q=0 in the structure of the formula (4), and number-average molecular weight Mn≈8,700.
The number-average molecular weight is a value measured using a gel permeation chromatography
(GPC) method and calculated using polymethyl methacrylate (PMMA) as a standard.
Analysis Conditions of Example 1
[0080] Analysis conditions of Example 1 are shown below.
1H NMR measurement method
Measurement apparatus: JNM-AL400 manufactured by JEOL Ltd.
Solvent: CDCl3 (TMS reference)
Components used in Example 2 and Comparative Examples
[0081] Components, other than the polysiloxane monomer of the present invention, used in
Example 2 and Comparative Examples are shown below.
∘Comparative compound of the formula (1)
PMPC: macromer having a phosphorylcholine functional group on a side chain (compound
of Experiment Example 4 of Patent Literature 8)
FM-7721: JNC Corporation, bi-terminal methacryloyloxypolydimethylsiloxane (molecular
weight≈5,000) ∘Other monomer
SiGMA: 2-hydroxy-3-(tris(trimethylsiloxy)silyl)propyl methacrylate
ES: 4-(2-hydroxyethyl)=1-[3-tris(trimethylsiloxy)silylpropyl]=2-methylidene succinate
TEGDMA: tetraethylene glycol dimethacrylate
oHydrophilic monomer
MPC: 2-(methacryloyloxyethyl)-2-(trimethylammonioethyl)phosphate
HPMA: hydroxypropyl methacrylate (a mixture of 2-hydroxypropyl ester and 2-hydroxy-1-methylethyl
ester, manufactured by Nippon Shokubai Co., Ltd.)
NVP: N-vinylpyrrolidone
HEMA: 2-hydroxyethyl methacrylate
DMAA: N,N-dimethylacrylamide
oSolvent
HexOH: hexanol
∘Initiator (polymerization initiator)
AIBN: 2,2'-azobis(isobutyronitrile) (10-hour half-life temperature: 65°C)
Evaluation methods in Example 2 are as described below.
(Surface Hydrophilicity (WBUT) of Contact Lens)
[0082] The surface hydrophilicity of a contact lens was evaluated on the basis of a water
film break up time (WBUT). Specifically, a contact lens ("film-shaped sample" in this
Example) was immersed in ISO saline overnight, and was lifted off the water surface
by holding its periphery with tweezers, and a period of time between the lifting from
the water surface and the breakup of a water surface on the lens surface (water surface
retention time) was measured. A state in which the water surface was broken up was
judged by visual observation. The measurement was performed 3 times, and the average
value thereof was determined. When the average value was 30 seconds or more, it was
judged that the surface hydrophilicity was satisfactory.
(Mechanical Strength of Contact Lens)
[0083] The modulus [MPa] of a contact lens was measured with a BAS-3305(W) breaking strength
analyzer manufactured by Yamaden Co., Ltd. in accordance with JIS-K7127, and its mechanical
strength was evaluated. Specifically, a sample obtained by cutting a contact lens
to a width of 2 mm was used and pulled at a speed of 1 mm/second with a distance between
two clamps being set to 6 mm, and the modulus was measured by detection with a 200
gf load cell. When the modulus was 0.3 MPa or more and 0.7 MPa or less, it was judged
that the mechanical strength was satisfactory.
(Oxygen Permeability of Contact Lens)
[0084] The oxygen permeability(Dk) of a sample obtained by stacking one to four contact
lenses together was measured in accordance with a measurement method based on a polarography
method described in ISO 18369-4. O2 Permeometer Model 201T of Rehder Development Company
was used for the measurement. The thickness of the lens(es) and a t/Dk value determined
by the measurement were plotted on the x-axis and the y-axis, respectively, and the
inverse of the slope of the regression line of the plot was defined as the oxygen
permeability (Dk) {(cm
2/sec)/(mLO
2/(mL×mmHg))}. A larger oxygen permeability(Dk) indicates more satisfactory oxygen
permeability. When the oxygen permeability(Dk) was 75 or more, it was judged that
the oxygen permeability was particularly satisfactory.
[Example 1-1]
[0085] In a 100 mL three-necked flask, 10.00 g of the silicone intermediate 1 (hydrosilyl
group-containing di-methacrylate-terminated silicone represented by the formula (4))
and 0.2140 g of the allyl group-containing phosphorylcholine compound represented
by the formula (5) were dissolved in 10.00 g of 2-propanol, and the solution was heated
to 80°C using an oil bath, followed by the addition of 40 µL of a 4 wt% solution of
hexachloroplatinic acid hexahydrate in 2-propanol.
[0086] A solution obtained by dissolving 1.93 g of the allyl group-containing phosphorylcholine
compound represented by the formula (5) in 5.78 g of 2-propanol was loaded into a
10 mL dropping funnel, which was attached to an upper part of the three-necked flask.
[0087] The solution in the dropping funnel was added dropwise over 30 minutes while the
mixture was kept at 80°C. After the dropwise addition, the mixture was subjected to
a reaction for an additional 1 hour under reflux. Low-boiling components were evaporated
under reduced pressure. After that, the residue was mixed with 33.18 g of ion-exchanged
water, 11.05 g of ethanol, and 44.21 g of ethyl acetate, and the whole was stirred.
After having been left to stand still, the mixture was separated into three layers.
The upper layer and the lower layer were discarded, and then reduced-pressure evaporation
from the middle layer under reduced pressure gave 7.31 g of a transparent gel-like
product. It was confirmed by
1H NMR analysis that the product was the compound represented by the formula (1).
1H NMR Analysis Values
[0088]
Peak area values for 2H of end double bonds at 5.54 ppm and 6.10 ppm (1.00+1.00=2.00)
An area value for 9H derived from a choline group at 3.34 ppm (46.89)
A peak area value derived from siloxane at 0.16 ppm (646.15)
[0089] Calculation from the above-mentioned values found the following: a≈108, b=5, c=1,
p=q=0, and X represents -CH
2CH
2- in the structural formula of the formula (1), and number-average molecular weight
Mn≈10,000. The number-average molecular weight is a value measured using a gel permeation
chromatography (GPC) method and calculated using polymethyl methacrylate (PMMA) as
a standard under the following measurement conditions.
Eluent: tetrahydrofuran
Flow rate: 0.8 mL/min
Column: three PLgel mixed-E columns (connected in series)
Column temperature: 40°C
Detector: differential refractometer
[Example 1-2 to Example 1-4, Comparative Example 1-1, and Comparative Example 1-2]
[0090] Example 1-2 to Example 1-4 were each performed in the same manner as Example 1-1
except that: the molecular weight and hydrosilyl group content ratio of the hydrosilyl
group-containing di-methacrylate-terminated silicone of the formula (4) were changed;
and the loading amount of the compound of the formula (5) was changed in proportion
to the concentration of hydrosilyl groups. The molar ratios of the constituent units
of the formula (1) in Example 1-1 to Example 1-4 and the calculation results of the
number-average molecular weights thereof are shown in Table 1.
Table 1
|
Example 1-1 |
Example 1-2 |
Example 1-3 |
Example 1-4 |
Compara tive Example 1-1 |
Compara tive Example 1-2 |
Formula (1) "a" |
108 |
20 |
500 |
52 |
600 |
10 |
Formula (1) "b" |
5 |
1 |
70 |
7 |
1 |
1 |
Formula (1) "c" |
1 |
1 |
1 |
1 |
1 |
1 |
Formula (1) "p" |
0 |
0 |
0 |
0 |
0 |
0 |
Formula (1) "q" |
0 |
0 |
0 |
0 |
0 |
0 |
Formula (1) X |
-CH2CH2- |
-CH2CH2- |
-CH2CH2- |
-CH2CH2- |
-CH2CH2- |
-CH2CH2- |
Number-average molecula r weight |
10,000 |
2,000 |
42,000 |
4,600 |
45,000 |
1,200 |
[Example 2-1]
[0091] 23.1 Parts by weight of MPC, 30.8 parts by weight of HPMA, 15.4 parts by weight of
the compound produced in Example 1, 30.8 parts by weight of NVP, 53.1 parts by weight
of SiGMA, 23.1 parts by weight of HexOH, 0.8 part by weight of TEGDMA, and 1.5 parts
by weight of AIBN were stirred and mixed at room temperature for 1 hour to be uniformly
dissolved to afford a monomer composition. Its composition is shown in Table 2.
[0092] 0.3 g of the monomer composition was poured into a cell measuring 25 mm×70 mm×0.2
mm obtained by interposing a polyethylene terephthalate sheet having a thickness of
0.1 mm as a spacer between two polypropylene plates, and the resultant was placed
in an oven. After the inside of the oven had been purged with nitrogen, the temperature
was increased to 100°C, and the temperature was kept for 2 hours to polymerize the
composition. Thus, a polymer was obtained.
[0093] The polymer was purified by being immersed in 40 g of 2-propanol for 4 hours, and
then immersed in 50 g of ion-exchanged water for 4 hours to remove an unreacted material
and the like. Further, the polymer was immersed in saline described in ISO-18369-3
to give a transparent film-shaped sample. The composition uniformity, polymerizability,
polymerization product transparency, and hydrogel transparency of the sample were
observed, and as a result, were each found to be satisfactory as shown in Table 2.
The water content of the sample was measured, and the result was as shown in Table
2. The composition uniformity was checked by visually observing the monomer composition
placed in a colorless and transparent container. For the polymerizability, the properties
of a polymerization product obtained by polymerizing the monomer composition were
checked by visual observation. For the polymerization product transparency, the transparency
of the polymerization product obtained by polymerizing the monomer composition was
checked by visual observation. For the hydrogel transparency, the transparency of
a hydrogel obtained by swelling the polymerization product, obtained by polymerizing
the monomer composition, in saline described in ISO-18369-3 was checked by visual
observation. The water content was measured by a technique described in ISO-18369-4.
Specifically, a hydrogel in an equilibrium water-containing state was dried, and its
water content was calculated from a difference between weights before and after drying.
[0094] The surface hydrophilicity and mechanical strength of the film-shaped sample were
evaluated by the above-mentioned methods. The results are shown in Table 2.
[0095] The oxygen permeability(Dk) of the film-shaped sample was evaluated by the above-mentioned
method. The result is shown in Table 2.
[Example 2-2 to Example 2-7]
[0096] Example 2-2 to Example 2-7 were each performed in the same manner as in Example 2-1
except that a composition shown in Table 2 was adopted. The results of evaluations
of composition uniformity (○: transparent, ×: clouded or precipitated), polymerizability
(○: solid, ×: viscous matter or liquid), polymerization product transparency (○: transparent,
×: clouded), hydrogel transparency (○: transparent, ×: clouded), water content, surface
hydrophilicity, mechanical strength, and oxygen permeability(Dk) performed in the
same manner as in Example 2-1 are shown in Table 2.
[Comparative Example 2-1]
[0097] Stirring and mixing were performed at room temperature in the same manner as in Example
2-1 except that, as shown in Table 3, 15.4 parts by weight of the compound of Comparative
Example 1-1 was used in place of 15.4 parts by weight of the compound represented
by the formula (1). However, a uniform solution was not obtained.
[Comparative Example 2-2]
[0098] A monomer composition was obtained through uniform dissolution by stirring and mixing
for 1 hour in the same manner as in Example 2-1 except that, as shown in Table 3,
15.4 parts by weight of the compound of Comparative Example 1-2 was used in place
of 15.4 parts by weight of the compound represented by the formula (1).
[Comparative Example 2-3]
[0099] Stirring and mixing were performed at room temperature in the same manner as in Example
2-1 except that, as shown in Table 3, 15.4 parts by weight of FM-7721 represented
by the formula (4) was used in place of 15.4 parts by weight of the compound represented
by the formula (1). However, a uniform solution was not obtained.
[Comparative Example 2-4]
[0100] A monomer composition was obtained through uniform dissolution by stirring and mixing
for 1 hour in the same manner as in Example 2-1 except that, as shown in Table 3,
15.4 parts by weight of PMPC was used in place of 15.4 parts by weight of the compound
represented by the formula (1).
Table 2
Kind |
Raw material |
Example 2-1 |
Example 2-2 |
Example 2-3 |
Example 2-4 |
Example 2-5 |
Example 2-6 |
Example 2-7 |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part (s) by weight |
Mixing ratio |
Part (s) by weight |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part(s) by weight |
Compound of formula (1) |
Example 1-1 |
10 |
15.4 |
|
|
|
|
|
|
10 |
15.4 |
|
|
10 |
15.4 |
Example 1-2 |
|
|
10 |
15.4 |
|
|
|
|
|
|
|
|
|
|
Example 1-3 |
|
|
|
|
20 |
30.8 |
|
|
|
|
20 |
30.8 |
|
|
Example 1-4 |
|
|
|
|
|
|
50 |
55.6 |
|
|
|
|
|
|
Comparative Example 1-1 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Comparative Example 1-2 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Comparative compound of formula (1) |
PMPC |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
FM-7721 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hydrophilic monomer |
MPC |
15 |
23.1 |
15 |
23.1 |
15 |
23.1 |
5 |
5.6 |
15 |
23.1 |
15 |
23.1 |
15 |
23.1 |
HPMA |
20 |
30.8 |
20 |
30.8 |
10 |
15.4 |
5 |
5.6 |
20 |
30.8 |
|
|
20 |
30.8 |
NVP |
20 |
30.8 |
20 |
30.8 |
20 |
30.8 |
30 |
33.3 |
20 |
30.8 |
20 |
30.8 |
|
|
HEMA |
|
|
|
|
|
|
|
|
|
|
10 |
15.4 |
|
|
DMAA |
|
|
|
|
|
|
|
|
|
|
|
|
20 |
30.8 |
Subtotal of monomers |
- |
65 |
100.0 |
65 |
100.0 |
65 |
100.0 |
90 |
100.0 |
65 |
100.0 |
65 |
100.0 |
65 |
100.0 |
Other monomer |
SiGMA |
34.5 |
53.1 |
34.5 |
53.1 |
34.5 |
53.1 |
9.5 |
10.6 |
|
|
34.5 |
53.1 |
|
|
ES |
|
|
|
|
|
|
|
|
34.5 |
53.1 |
|
|
34.5 |
53.1 |
TEGDMA |
0.5 |
0.8 |
0.5 |
0.8 |
0.5 |
0.8 |
0.5 |
0.6 |
0.5 |
0.8 |
0.5 |
0.8 |
0.5 |
0.8 |
Total of monomers |
- |
100 |
|
100 |
|
100 |
|
100 |
|
100 |
|
100 |
|
100 |
|
Solvent |
HexOH |
15 |
23.1 |
20 |
30.8 |
20 |
30.8 |
20 |
22.2 |
10 |
15.4 |
20 |
30.8 |
10 |
15.4 |
Initiator |
AIBN |
1 |
1.5 |
1 |
1.5 |
1 |
1.5 |
1 |
1.1 |
1 |
1.5 |
1 |
1.5 |
1 |
1.5 |
Polymerizat ion step |
Temperature |
100°C |
100°C |
100°C |
100°C |
100°C |
100°C |
100°C |
Time |
2 hours |
2 hours |
2 hours |
2 hours |
2 hours |
2 hours |
2 hours |
Evaluation item |
Evaluation result |
Composition uniformity |
○ |
○ |
○ |
○ |
○ |
○ |
○ |
Polymerizability |
○ |
○ |
○ |
○ |
○ |
○ |
○ |
Polymerization product transparency |
○ |
○ |
○ |
○ |
○ |
○ |
○ |
Hydrogel transparency |
○ |
○ |
○ |
○ |
○ |
○ |
○ |
WBUT [s] |
>30 |
>30 |
>30 |
>30 |
>30 |
>30 |
>30 |
Water content [%] |
55 |
45 |
60 |
40 |
50 |
55 |
45 |
Modulus [MPa] |
0.5 |
0.7 |
0.4 |
0.7 |
0.6 |
0.6 |
0.7 |
Oxygen permeability(Dk) |
80 |
100 |
75 |
100 |
90 |
80 |
100 |
Table 3
Kind |
Raw material |
Comparative Example 2-1 |
Comparative Example 2-2 |
Comparative Example 2-3 |
Comparative Example 2-4 |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part(s) by weight |
Mixing ratio |
Part(s) by weight |
Compound of formula (1) |
Example 1-1 |
|
|
|
|
|
|
|
|
Example 1-2 |
|
|
|
|
|
|
|
|
Example 1-3 |
|
|
|
|
|
|
|
|
Example 1-4 |
|
|
|
|
|
|
|
|
Comparative Example 1-1 |
10 |
15.4 |
|
|
|
|
|
|
Comparative Example 1-2 |
|
|
10 |
15.4 |
|
|
|
|
Comparative compound of formula (1) |
PMPC |
|
|
|
|
|
|
10 |
15.4 |
FM-7721 |
|
|
|
|
10 |
15.4 |
|
|
Hydrophilic monomer |
MPC |
15 |
23.1 |
15 |
23.1 |
15 |
23.1 |
15 |
23.1 |
HPMA |
20 |
30.8 |
20 |
30.8 |
20 |
30.8 |
20 |
30.8 |
NVP |
20 |
30.8 |
20 |
30.8 |
20 |
30.8 |
20 |
30.8 |
HEMA |
|
|
|
|
|
|
|
|
DMAA |
|
|
|
|
|
|
|
|
Subtotal of monomers |
- |
65 |
100.0 |
65 |
100.0 |
65 |
100.0 |
65 |
100.0 |
Other monomer |
SiGMA |
34.5 |
53.1 |
34.5 |
53.1 |
34.5 |
53.1 |
34.5 |
53.1 |
ES |
|
|
|
|
|
|
|
|
TEGDMA |
0.5 |
0.8 |
0.5 |
0.8 |
0.5 |
0.8 |
0.5 |
0.8 |
Total of monomers |
- |
100 |
|
100 |
|
100 |
|
100 |
|
Solvent |
HexOH |
15 |
23.1 |
15 |
23.1 |
15 |
23.1 |
15 |
23.1 |
Initiator |
AIBN |
1 |
1.5 |
1 |
1.5 |
1 |
1.5 |
1 |
1.5 |
Polymerizat ion step |
Temperature |
100°C |
100°C |
100°C |
100°C |
Time |
2 hours |
2 hours |
2 hours |
2 hours |
Evaluation item |
Evaluation result |
Composition uniformity |
× |
○ |
× |
○ |
Polymerizability |
The evaluation was stopped because uniform dissolution was not achieved. |
○ |
The evaluation was stopped because uniform dissolution was not achieved. |
○ |
Polymerization product transparency |
○ |
○ |
Hydrogel transparency |
○ |
○ |
WBUT [s] |
>30 |
>30 |
Water content [%] |
40 |
55 |
Modulus [MPa] |
2.4 |
0.5 |
Oxygen permeability(Dk) |
80 |
60 |
[0101] As apparent from the results of Table 2 and Table 3, in each of Example 2-1 to Example
2-7, Comparative Example 2-2, and Comparative Example 2-4, the WBUT evaluation was
more than 30 seconds, indicating satisfactory surface hydrophilicity.
[0102] Meanwhile, in each of Comparative Example 2-1 and Comparative Example 2-3, a uniform
composition was unable to be obtained.
[0103] In each of Example 2-1 to Example 2-7 and Comparative Example 2-4, the modulus fell
within the range of 0.3 MPa or more and 0.7 MPa or less, indicating satisfactory mechanical
strength.
[0104] Meanwhile, in Comparative Example 2-2, the modulus was 2.4, and hence the mechanical
strength was inappropriate for a soft contact lens.
[0105] In each of Example 2-1 to Example 2-7 and Comparative Example 2-2, the oxygen permeability(Dk)
was 75 or more, indicating a particularly satisfactory oxygen permeability(Dk).
[0106] Meanwhile, in Comparative Example 2-4, the oxygen permeability(Dk) was 60, and hence
the oxygen permeability(Dk) was unsatisfactory. In Comparative Example 2-4, PMPC having
a structure similar to the formula (1) was used in place of the compound represented
by the formula (1), and the above-mentioned result was able to confirm that it was
difficult to increase the oxygen permeability of a contact lens produced with a monomer
other than the formula (1).
[0107] Thus, it was confirmed that the polymer obtained by polymerizing the monomer composition
containing the polysiloxane monomer represented by the formula (1) was capable of
producing a soft contact lens having satisfactory surface hydrophilicity, appropriate
mechanical strength, and a satisfactory oxygen permeability(Dk).
[0108] As described above, it was confirmed that the phosphorylcholine group-containing
polysiloxane monomer of the present invention simultaneously satisfied surface hydrophilicity,
appropriate mechanical strength, and oxygen permeability when copolymerized with a
polymerizable monomer, such as a hydrophilic monomer, and hence was useful as a polysiloxane
monomer to be used as a raw material for an ophthalmic device.
Industrial Applicability
[0109] The polysiloxane monomer having a phosphorylcholine group, which simultaneously satisfies
surface hydrophilicity, appropriate mechanical strength, and oxygen permeability when
copolymerized with a polymerizable monomer, such as a hydrophilic monomer, and which
is used as a raw material for an ophthalmic device, can be provided.